Resumes
Resumes
![Erik Roggeman Photo 1 Erik Roggeman Photo 1](/img/not-found.png)
Director - Quality Assurance
View pageLocation:
Elmhurst, IL
Industry:
Pharmaceuticals
Work:
Eli Lilly and Company
Director - Quality Assurance
Eli Lilly and Company Dec 2011 - Mar 2013
Manager - Quality Assurance
Eli Lilly and Company Dec 2008 - Nov 2011
Associate Quality Consultant
Eli Lilly and Company Apr 2004 - Nov 2008
Associate Technical Consultant
Ibm Sep 1, 1998 - Dec 31, 2004
Senior Process Engineer
Director - Quality Assurance
Eli Lilly and Company Dec 2011 - Mar 2013
Manager - Quality Assurance
Eli Lilly and Company Dec 2008 - Nov 2011
Associate Quality Consultant
Eli Lilly and Company Apr 2004 - Nov 2008
Associate Technical Consultant
Ibm Sep 1, 1998 - Dec 31, 2004
Senior Process Engineer
Education:
University of Notre Dame 1996 - 1998
Master of Science, Masters, Chemical Engineering Rose - Hulman Institute of Technology 1992 - 1996
Bachelors, Bachelor of Science, Chemical Engineering York Community High School
Master of Science, Masters, Chemical Engineering Rose - Hulman Institute of Technology 1992 - 1996
Bachelors, Bachelor of Science, Chemical Engineering York Community High School
Skills:
Validation
Gmp
Change Control
Pharmaceutical Industry
Capa
Fda
Computer System Validation
Quality Assurance
Technology Transfer
21 Cfr Part 11
Gxp
V&V
Six Sigma
Quality Auditing
Quality System
Analytical Chemistry
Chemistry
Root Cause Analysis
Chromatography
Quality Management
Process Improvement
Sop
Hplc
Quality Control
Biotechnology
Cross Functional Team Leadership
Drug Development
Gamp
Aseptic Processing
Spc
R&D
Clinical Trials
Biopharmaceuticals
Project Management
Process Optimization
Process Simulation
Lifesciences
Manufacturing
Regulatory Submissions
Operational Excellence
Design of Experiments
Clinical Development
Fmea
Lean Manufacturing
Process Engineering
Process Control
Iso 13485
Cleaning Validation
Lims
Gas Chromatography
Gmp
Change Control
Pharmaceutical Industry
Capa
Fda
Computer System Validation
Quality Assurance
Technology Transfer
21 Cfr Part 11
Gxp
V&V
Six Sigma
Quality Auditing
Quality System
Analytical Chemistry
Chemistry
Root Cause Analysis
Chromatography
Quality Management
Process Improvement
Sop
Hplc
Quality Control
Biotechnology
Cross Functional Team Leadership
Drug Development
Gamp
Aseptic Processing
Spc
R&D
Clinical Trials
Biopharmaceuticals
Project Management
Process Optimization
Process Simulation
Lifesciences
Manufacturing
Regulatory Submissions
Operational Excellence
Design of Experiments
Clinical Development
Fmea
Lean Manufacturing
Process Engineering
Process Control
Iso 13485
Cleaning Validation
Lims
Gas Chromatography